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1 that specifically degrade heparan sulfate, a sulfated glycosaminoglycan.
2 K is promoted by chondroitin sulfate (CS), a sulfated glycosaminoglycan.
3 PKR is also activated by heparin, a highly sulfated glycosaminoglycan.
4 ild-type PrP, as well as by treatment with a sulfated glycosaminoglycan.
5 osomal sulfatases involved in degradation of sulfated glycosaminoglycans.
6 specimens were immunoprobed for lubricin and sulfated glycosaminoglycans.
7 specimens were immunoprobed for lubricin and sulfated glycosaminoglycans.
8 6T leads to a significant depletion of tumor-sulfated glycosaminoglycans.
9 the granzyme from serglycin to immobilized, sulfated glycosaminoglycans.
10 seases resulting from impaired catabolism of sulfated glycosaminoglycans.
11 f histones with type IV collagen and heparan-sulfated glycosaminoglycans.
12 fect of heparin was mimicked by a variety of sulfated glycosaminoglycans.
15 cell surface CD44 and aggrecan and deposit a sulfated glycosaminoglycan and cartilage-specific collag
16 osition of AF-specific extracellular matrix (sulfated glycosaminoglycan and collagen type I), indicat
17 g was associated with increased synthesis of sulfated glycosaminoglycans and augmented expression of
18 ned by our demonstrated N6L interaction with sulfated glycosaminoglycans and consequently the control
20 assays, granzyme B was found to exchange to sulfated glycosaminoglycans and, depending on the cell t
21 ith biochemical and histological analyses of sulfated glycosaminoglycans, and x-ray attenuation was f
24 ctional interaction between antithrombin and sulfated glycosaminoglycans can be regulated by osmotic
27 and that this adhesion event depends on the sulfated glycosaminoglycan chains of the proteoglycans.
28 result from differences in intracellular HA, sulfated glycosaminoglycan concentration, apoptosis, or
31 riments (BIAcore) determined that DMAV binds sulfated glycosaminoglycans (e.g. heparin, KD ~100 nmol/
32 d previously that heparan sulfate, a type of sulfated glycosaminoglycan, facilitates neutrophil recru
33 ctions of HSPGs are mediated by the variable sulfated glycosaminoglycan (GAG) chains attached to a co
40 ggrecanase activity requires the presence of sulfated glycosaminoglycans (GAGs) attached to the aggre
42 y langerin was demonstrated to interact with sulfated glycosaminoglycans (GAGs), in a Ca(2+)-independ
43 importance of tissue-specifically expressed, sulfated glycosaminoglycans (GAGs), like HS, in determin
47 ells were deficient in the expression of the sulfated glycosaminoglycans heparan sulfate and chondroi
50 We herein show, for the first time, that sulfated glycosaminoglycans, heparin, heparan sulfate (H
51 ed by 36 and 30%, respectively, and SDC4 and sulfated glycosaminoglycan in the culture medium were in
52 itical role for both cellular activation and sulfated glycosaminoglycans in adherence of H. somnus to
54 harides, such as sialyl Lewis(x), as well as sulfated glycosaminoglycan-like epitopes can be readily
56 this study, we have evaluated the effect of sulfated glycosaminoglycans on the invasion of erythrocy
57 es with xanthine oxidase (XO) for binding to sulfated glycosaminoglycans, or the XO inhibitor allopur
58 g of CpClec-Fc was specifically inhibited by sulfated glycosaminoglycans, particularly heparin and he
59 apted to achieve the separation of the major sulfated glycosaminoglycans produced by cells in culture
63 d compressive moduli as well as collagen and sulfated glycosaminoglycan (sGAG) content also vary with
64 atants, and tissue extracts were assayed for sulfated glycosaminoglycan (sGAG) content and analyzed b
67 TNFalpha, interleukin-1beta (IL-1beta), and sulfated glycosaminoglycans (sGAG) in synovial fluid (SF
69 ident with a significant decrease in scleral sulfated glycosaminoglycan synthesis rates in treated ey
71 IMP-3 K26A/K45A retained higher affinity for sulfated glycosaminoglycans than K42A/K110A and exhibite
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